Pharmaceutical

URIC ACID

  • CAS:69-93-2
  • purity:99%
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Cost-effective and customizable URIC ACID 69-93-2 factory

  • Molecular Formula: C5H4N4O3
  • Molecular Weight: 168.112
  • Appearance/Colour: Off-white crystals 
  • Vapor Pressure: 2.63E-31mmHg at 25°C 
  • Melting Point: >300°C(lit.) 
  • Refractive Index: 1.721 
  • Boiling Point: 863 °C at 760 mmHg 
  • PKA: 3.89(at 12℃) 
  • Flash Point: 475.7 °C 
  • PSA: 114.37000 
  • Density: 1.87 g/cm3 
  • LogP: -1.76720 

URIC ACID(Cas 69-93-2) Usage

Properties and Preparation

Uric acid is a colorless, odorless and tasteless solid with molecular formula C5H4N4O3. It is largely insoluble in water (60 mg/L, at 20 °C)[2]. It is soluble in 1 M NaOH (50 mg/ml)[3]. Rather than melt, it decomposes in air above 250°C. Uric acid is produced from purines by the enzyme xanthine oxidase via the purine metabolism pathway. In the majority of mammals, uric acid is further degraded to allantoin via the urate oxidase (uricase) enzyme. Allantoin is then freely excreted from the body in the urine. Humans, apes, and certain New World monkeys have higher uric acid levels compared with other mammals[4]. Commercially, uric acid has been prepared from guano, which is essentially the droppings of bats or seabirds. Large quantities of guano can be found on some islands. Uric acid can be produced via extracting guano with alkali and then precipitating with acid[5][6].

Biochem/physiol Actions

Uric acid is an insoluble catabolite produced by adenine and guanine metabolism. Accumulation of uric acid leads to gout, hyperuricemia, arthritis and renal failure. Elevated uric acid levels contributes to hypertension and pathogenesis of cardiovascular disease. Low uric acid levels associated with Parkinson′s disease and multiple sclerosis, may elicit protective functionality. High levels of uric acid in patients with chronic obstructive pulmonary disease (COPD) may serve as potential marker for diagnosis.

Safety Profile

Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Crystallise uric acid from hot distilled H2O (the solubility in H2O is 1part/39,000parts at 18o and 1part/2,000parts at 100o). It is best purified by dissolving in an alkaline solution and acidifying with dilute HCl and drying it at 100o in a vacuum. [Bergmann & Dikstein J Am Chem Soc 77 691 1955, Lister Purines Part II, Fused Pyrimidines Brown Ed, Wiley-Interscience pp256-257 1971, ISBN 0-471-38205-1, Beilstein 26 H 513, 26 I 151, 26 II 293, 26 III/IV 2619.]

Introduction

Uric acid is a breakdown substance of purines which exist in body tissues and some food and drinks. Purines are a type of chemical compound in nature consisted in nucleic acids (DNA and RNA). Uric acid is created in the body via purine metabolism and circulated within the bloodstream, and it will be excreted in urine as waste. As a result, there is a certain balanced amount of uric acid in the bloodstream, which is of great importance to the functions of body[1]. Uric acid is composed in the form of urate of ammonia, and it is the primary constituent of the urine of birds and reptiles. Uric acid helps to keep the birds' weight down which is crucial for their flight. Due to its acidic properties, uric acid from birds does damage paints on cars. Insects produce uric acid during protein catabolism. In addition, uric acid helps to make butterflies iridescent. Its crystals also reflect the light produced in fireflies by bioluminescence[2].

Definition

A nitrogen compound produced from purines. In certain animals (e.g. birds and reptiles), it is the main excretory product resulting from breakdown of amino acids. In humans, uric acid crystals in the joints are the cause of gout.

InChI:InChI=1/C5H4N4O3/c10-3-1-2(7-4(11)6-1)8-5(12)9-3/h(H4,6,7,8,9,10,11,12)

69-93-2 Relevant articles

-

Horbaczewski

, p. 202,584 (1887)

-

The hunt for 8-oxoguanine deaminase

Hall, Richard S.,Fedorov, Alexander A.,Marti-Arbona, Ricardo,Fedorov, Elena V.,Kolb, Peter,Sauder, J. Michael,Burley, Stephen K.,Shoichet, Brian K.,Almo, Steven C.,Raushel, Frank M.

, p. 1762 - 1763 (2010)

(Chemical Equation Presented) An enzyme ...

Xanthine dehydrogenase electrocatalysis: Autocatalysis and novel activity

Kalimuthu, Palraj,Leimkühler, Silke,Bernhardt, Paul V.

, p. 2655 - 2662 (2011)

The enzyme xanthine dehydrogenase (XDH) ...

Mixed Inhibition of the Oxidoreductase Activity of Xanthine Oxidase by Pd2+ Ion

Sau, Apurba Kumar,Mondal, Madhu Sudan,Mitra, Samaresh

, p. 1547 - 1548 (1994)

Pd2+ ion shows 100percent inhibition of ...

Low-potential amperometric enzyme biosensor for xanthine and hypoxanthine

Kalimuthu, Palraj,Leimkühler, Silke,Bernhardt, Paul V.

, p. 10359 - 10365 (2012)

The bacterial xanthine dehydrogenase (XD...

-

Horbaczewski

, p. 221 (1891)

-

Tetrathiatriarylmethyl radical with a single aromatic hydrogen as a highly sensitive and specific superoxide probe

Liu, Yangping,Song, Yuguang,De Pascali, Francesco,Liu, Xiaoping,Villamena, Frederick A.,Zweier, Jay L.

, p. 2081 - 2091 (2012)

Superoxide (O2?-) plays crucial roles in...

Bioluminescence Detection of Superoxide Anion Using Aequorin

Rahmani, Hossein,Ghavamipour, Fahimeh,Sajedi, Reza H.

, p. 12768 - 12774 (2019)

Although the superoxide anion (O2 -·) is...

Inhibition studies of bovine xanthine oxidase by luteolin, silibinin, quercetin, and curcumin

Pauff, James M.,Hille, Russ

, p. 725 - 731 (2009)

Xanthine oxidoreductase (XOR) is a molyb...

Effects of zinc acexamate (NAS-501) on superoxide radicals and lipid peroxidation of rat gastric mucosa

Tsutsui, Yasuhiro,Nakamura, Yukio,Yamaguchi, Shiho,Kawanaka, Nobuyo,Sato, Makoto

, p. 209 - 219 (1999)

Zinc acexamate (NAS-501), an anti-ulcer ...

-

Horbaczewski

, p. 356 ()

-

A new method for the assay of xanthine oxidase activity

Sugiura,Kato,Adachi,Ito,Hirano

, p. 430 - 432 (1981)

-

Kinetic model of oxidation catalyzed by xanthine oxidase - The final enzyme in degradation of purine nucleosides and nucleotides

Banach, Kinga,Bojarska, Elzbieta,Kazimierczuk, Zygmunt,Magnowska, Lucyna,Bzowska, Agnieszka

, p. 465 - 469 (2005)

A new kinetic model is presented for ana...

Inhibition of xanthine oxidase by flavonoids.

Nagao,Seki,Kobayashi

, p. 1787 - 1790 (1999)

Various dietary flavonoids were evaluate...

-

Horbaczewski

, p. 201 (1887)

-

Behavior of some purine derivatives towards xanthine oxidase

Werner,Kapoor

, p. 308 - 309 (1966)

-

Hydrogen peroxide is the major oxidant product of xanthine oxidase

Kelley, Eric E.,Khoo, Nicholas K.H.,Hundley, Nicholas J.,Malik, Umair Z.,Freeman, Bruce A.,Tarpey, Margaret M.

, p. 493 - 498 (2010)

Xanthine oxidase (XO) is a critical sour...

Pd nanoparticles supported on nitrogen, sulfur-doped three-dimensional hierarchical nanostructures as peroxidase-like catalysts for colorimetric detection of xanthine

Shi, Weijie,Fan, Hai,Ai, Shiyun,Zhu, Lusheng

, p. 32183 - 32190 (2015)

Pd nanoparticles supported on nitrogen, ...

Structure-activity relationship of xanthones as inhibitors of xanthine oxidase

Zhou, Ling-Yun,Peng, Jia-Le,Wang, Jun-Ming,Geng, Yuan-Yuan,Zuo, Zhi-Li,Hua, Yan

, (2018/02/17)

Polygala plants contain a large number o...

Tissue metabolomic profiling to reveal the therapeutic mechanism of reduning injection on LPS-induced acute lung injury rats

Xiong, Zhili,Weng, Yanmin,Lang, Lang,Ma, Shuping,Zhao, Longshan,Xiao, Wei,Wang, Yanjuan

, p. 10023 - 10031 (2018/03/23)

Acute lung injury (ALI) is a severe resp...

Real-Time Monitoring of Enzyme-Catalysed Reactions using Deep UV Resonance Raman Spectroscopy

Westley, Chloe,Fisk, Heidi,Xu, Yun,Hollywood, Katherine A.,Carnell, Andrew J.,Micklefield, Jason,Turner, Nicholas J.,Goodacre, Royston

, p. 6983 - 6987 (2017/05/29)

For enzyme-catalysed biotransformations,...

69-93-2 Process route

N-(guanin-C<sup>8</sup>-yl)-1-naphthylamine
80156-61-2

N-(guanin-C8 -yl)-1-naphthylamine

uric Acid
69-93-2

uric Acid

1-amino-naphthalene
134-32-7

1-amino-naphthalene

Conditions
Conditions Yield
With alkali;
xanthin
69-89-6,6053-41-4

xanthin

pyrimidine-2,4,5,6(1H,3H)-tetraone
61066-33-9,61066-34-0,61066-35-1,61127-23-9

pyrimidine-2,4,5,6(1H,3H)-tetraone

uric Acid
69-93-2

uric Acid

urea
57-13-6

urea

Conditions
Conditions Yield
at 25 ℃; Product distribution; Mechanism; Rate constant; electrochemical oxidation; buffer (pH=2-6); various times, potentials and electrodes;

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